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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354572Generated: October 27, 2026

Acetyl chloride → 6-(2,4-Dichlorophenyl)-2-oxo-5-hexene-4-yl Acetate

https://huagongshe.com/reaction/354572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant6-(2,4-Dichlorophenyl)-4-hydroxy-5-hexene-2-oneHCID 54359312—
SolventPyridineHCID 1049—
Product6-(2,4-Dichlorophenyl)-2-oxo-5-hexene-4-yl AcetateHCID 5446766787.4%

Reaction Conditions

Temperature20 °C

Reaction Steps

Acetyl chloride (1.2 ml, 16.5 mmole) was added dropwise to a stirred solution of 6-(2,4-dichlorophenyl)-4-hydroxy-5-hexene-2-one (3.9 g, 15 mmole) in pyridine (60 ml) at 0° C. The ice bath was removed, and the reaction mixture was stirred at 20° C. for 2 hours and then diluted with ether (300 ml). The ether solution was washed with 1 N HCl (3×300 ml) and saturated NaHCO3, dried over MgSO4, filtered and evaporated. The residual pale amber oil (4.1 g) was chromatographed on a 50 mm column with 15 cm of silica gel (230-400 mesh). Elution with methylene chloride (2 L) provided the title compound as a pale yellow oil (3.95 g, 87%): pmr (CDCl3) δ2.03 (3H, s), 2.17 (3H, s), 2.83 (2H, dd).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04375475
Source datasetuspto-grants-1983_03
ORD IDord-a8e5684d54fc4ed9846617a6e8fc6b01
Source noteuspto-grants-1983_03